1. CTLA-4 Regulates Induction of Anergy In Vivo
Rebecca J. Greenwald, Vassiliki A. Boussiotis, Robert B. Lorsbach, Abul K. Abbas, Arlene H. Sharpe 
Immunity 
Volume 14, Issue 2, Pages (February 2001)
DOI: /S (01)

2. Figure 1
DO11+ RAG2−/− and DO11+ RAG2−/−CTLA-4−/− T Cells Exhibit a Naive Phenotype and Respond Comparably to Antigen
Lymph node cells were harvested from unstimulated DO11+ RAG2−/− and DO11+ RAG2−/−CTLA-4−/− mice, CD4+ T cells were purified from cell suspensions, and CD4+ T cells were stained for the DO11.10 TCR with the clonotypic antibody KJ1-26 and CD4 and analyzed by flow cytometry. The percentage of KJ1-26+ CD4+ T cells is indicated on the FACS plot. Purified CD4+ T cells were stained for CD4 and either CD25 or CD62L. The percentages of double-positive cells are indicated (+/+ and −/− denote CTLA-4 genotype). (B) CD4+ T cells from DO11+ RAG2−/− and DO11+ RAG2−/−CTLA-4−/− were cultured with OVA323–339 and APCs for 4 days and restimulated for 3 days, then stained for KJ1-26, CD4, and CD25 or CD62L. The histogram plots represent cells gated on the KJ1-26+ CD4+ population (filled histogram is CD25 or CD62L staining; dashed line is isotype-matched control). The results are representative of three experiments with two to three mice per group
Immunity  , DOI: ( /S (01) )

3. Figure 2
Levels of Proliferation and Effector Cytokines Are Elevated during the Secondary Responses of DO11+ RAG2−/−CTLA-4−/− T Cells to Antigen Stimulation
(A–B) DO11+ RAG2−/− (closed circles) (denoted as +/+ to indicate CTLA-4 genotype) or DO11+ RAG2−/−CTLA-4−/−(open squares) (denoted as −/− to indicate CTLA-4 genotype) T cells were purified and cultured with mitomycin-C-treated APCs and OVA323–339 for 4 days. Proliferation was measured by 3[H]thymidine incorporation during the primary response at day 4 (A) and during the secondary response at day 3 (B) at the indicated peptide concentrations.
(C) Cytokine secretion was detected by ELISA of culture supernatants in the primary at days 1–4 and in the secondary at days 1–3 after stimulation with 1.0 μg/ml of OVA peptide. Cells cultured in the absence of peptide did not secrete measurable cytokines (data not shown). The error bars represent standard deviations. These results are representative of three experiments
Immunity  , DOI: ( /S (01) )

4. Figure 3
Activation-Induced Cell Death Is Comparable in DO11+ RAG2−/− and DO11+ RAG2−/−CTLA-4−/− T Cells
DO11+ RAG2−/− (closed circles) or DO11+ RAG2−/−CTLA-4−/− (open squares) T cells were purified and cultured with mitomycin-C-treated APCs with OVA323–339 (1.0 μg/ml) for 4 days. T cells were rested overnight with IL-2, and viable cells were cultured with IL-2 and varying concentrations of plate-bound anti-CD3 (0–1.0 μg/ml). After 24 hr, cell death was assessed by FACS analysis, which was indicated as propidium iodide incorporation by CD4+ T cells. The error bars represent standard deviations for triplicate samples. The results are representative of three experiments
Immunity  , DOI: ( /S (01) )

5. Figure 4
Expansion of DO11+ RAG2−/−CTLA-4−/− T Cells Is Greater Than DO11+ RAG2−/− T Cells In Vivo
DO11+ RAG2−/− were adoptively transferred into wt recipients and either untreated (naive), immunized subcutaneously with 50 μg OVA323–339 peptide in IFA (primed), or given 300 μg OVA323–339 in PBS intravenously (tolerized). At 4 and 7 days after treatment, draining lymph node cells were harvested, cell suspensions pooled for each group, and CD4+ T cells purified. A portion of the CD4+ T cells were stained with KJ1-26 and CD4 to measure antigen-specific T cell expansion in vivo and analyzed by flow cytometry. One representative experiment of three, using three to five mice per treatment group, is shown. The percentage of KJ1-26+ CD4+ T cells is indicated on the FACS plots. (Mean percent expansion of KJ1-26+ CD4+ T cells in vivo. [Day 4] DO11+ RAG2−/−: naive = 0.53 ± 0.05, primed = 6.2 ± 1.2, and tolerized = 3.9 ± 0.92; DO11+ RAG2−/−CTLA-4−/−: naive = 0.57 ± 0.17, primed = 14 ± 5.1, and tolerized = 8.6 ± [Day 7] DO11+ RAG2−/−: naive = 0.38 ± 0.13, primed = 9.0 ± 0.81, and tolerized = 1.1 ± 0.36; DO11+ RAG2−/−CTLA-4−/−: naive = 0.55 ± 0.05, primed = ± 1.55, and tolerized = 2.61 ± 0.21.) The mean and standard deviations represent the average values for three experiments
Immunity  , DOI: ( /S (01) )

6. Figure 5
DO11+ RAG2−/−CTLA-4−/− T Cells Are Resistant to Tolerance Induction In Vivo
DO11+ RAG2−/− and DO11+ RAG2−/−CTLA-4−/− were adoptively transferred and treated (naive, primed, and tolerized) 1 day later. Lymph nodes were harvested at days 4 and 7 after treatment. KJ1-26+ CD4+ T cells were cultured with wild-type mitomycin-C-treated APCs and OVA323–339 peptide. Proliferation was measured at day 3 of restimulation for DO11+ RAG2−/− (closed circles) or DO11+ RAG2−/−CTLA-4−/− (open squares) over a range of peptide doses (0–1.0 μg/ml). IL-2 production was detected from culture supernatants on days 1–3 for each treatment group restimulated with 1.0 μg/ml of peptide. Each time point reflects the mean of triplicate samples, and error bars represent standard deviations. One representative experiment of three, using three to five mice per treatment group, is shown
Immunity  , DOI: ( /S (01) )

7. Figure 5
DO11+ RAG2−/−CTLA-4−/− T Cells Are Resistant to Tolerance Induction In Vivo
DO11+ RAG2−/− and DO11+ RAG2−/−CTLA-4−/− were adoptively transferred and treated (naive, primed, and tolerized) 1 day later. Lymph nodes were harvested at days 4 and 7 after treatment. KJ1-26+ CD4+ T cells were cultured with wild-type mitomycin-C-treated APCs and OVA323–339 peptide. Proliferation was measured at day 3 of restimulation for DO11+ RAG2−/− (closed circles) or DO11+ RAG2−/−CTLA-4−/− (open squares) over a range of peptide doses (0–1.0 μg/ml). IL-2 production was detected from culture supernatants on days 1–3 for each treatment group restimulated with 1.0 μg/ml of peptide. Each time point reflects the mean of triplicate samples, and error bars represent standard deviations. One representative experiment of three, using three to five mice per treatment group, is shown
Immunity  , DOI: ( /S (01) )

8. Figure 6
Cell Cycling Is Greater in DO11+ RAG2−/−CTLA-4−/− T Cells Given a Tolerogenic Stimulus In Vivo
Division of CFSE-labeled DO11+ RAG2−/− (solid line) or DO11+ RAG2−/−CTLA-4−/− (dashed line) T cells after adoptive transfer into wt recipients. At day 3 following treatment (naive, primed, or tolerized), draining lymph nodes were collected. Cell suspensions were stained for CD4 and KJ1-26. Histograms represent CFSE expression gated on CD4+ KJ1-26+ T cells. These results are representative of three experiments
Immunity  , DOI: ( /S (01) )

9. Figure 7
DO11+ RAG2−/− but Not DO11+ RAG2−/−CTLA-4−/− T Cells Given a Tolerogenic Stimulus Are Arrested at the G1 Phase of the Cell Cycle
(A) Lysates from unstimulated DO11+ RAG2−/− and DO11+ RAG2−/−CTLA-4−/− T cells were analyzed by SDS-PAGE and immunoblotted with antiserum specific for p27kip1. Blots were stripped and reprobed with antiserum specific for cdk4 and cdk2.
(B) Following adoptive transfer of DO11+ RAG2−/− and DO11+ RAG2−/−CTLA-4−/− T cells and treatment (N, naive; P, primed; or T, tolerized), CD4+ KJ1-26+ T cells were restimulated with mitomycin-C-treated APCs and OVA peptide for 3 days. At day 3, lysates were prepared and analyzed by SDS-PAGE and immunoblotted with antiserum specific for cyclin D2, cdk4, or cdk2. To assay kinase activity, immunoprecipitations were performed with anti-cdk2-specific antiserum, and in vitro kinase reactions were done using histone H1 as exogenous substrate.
(C) The same immunoblots used in (B) were stripped and reprobed with monoclonal antibody specific for p27kip1.
(D) Lysates from the same samples described above (“unst,” unstimulated), were immunoblotted with monoclonal antibody specific for Rb. Densitometric values are provided on each blot. Results are representative of three experiments
Immunity  , DOI: ( /S (01) )